A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593354



Internal ID20966425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38818556..38819636hg38UCSC Ensembl
chr17:36974809..36975889hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381081
hg191081
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242888
Samples
Known GenesCWC25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593354
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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